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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT02541747
Other study ID # CG14114
Secondary ID
Status Completed
Phase Phase 4
First received June 20, 2015
Last updated July 9, 2016
Start date June 2014
Est. completion date June 2015

Study information

Verified date September 2015
Source Taichung Veterans General Hospital
Contact n/a
Is FDA regulated No
Health authority Taiwan: Ministry of Health and Welfare
Study type Interventional

Clinical Trial Summary

This study aims to evaluate the effects of aroma massage to sleep quality of the nurses and staff during night shift.


Description:

Night shift increases physical and psychological pressure, and even affects their sleep quality. This study aims to evaluate the effects of aroma massage to sleep quality of the nurses during night shift after life-style modification and/or aroma massage. The investigators adopt a Randomized Controlled Trial (RCT) in this study. The investigators expect aroma massage would improve the sleep quality during night shift.


Recruitment information / eligibility

Status Completed
Enrollment 77
Est. completion date June 2015
Est. primary completion date June 2015
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 20 Years to 65 Years
Eligibility Inclusion Criteria:

- Shift-Work Nurses and Staff

Exclusion Criteria:

- Diabetes mellitus, cardiovascular disease and psychological disorders

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Treatment


Related Conditions & MeSH terms


Intervention

Behavioral:
massage
massage

Locations

Country Name City State
Taiwan Division of Endocrinology and Metabolism, Department of Internal Medicine, Taichung Veterans General Hospital Taichang

Sponsors (1)

Lead Sponsor Collaborator
Taichung Veterans General Hospital

Country where clinical trial is conducted

Taiwan, 

Outcome

Type Measure Description Time frame Safety issue
Primary brain-derived neurotrophic factor 4 weeks No
Secondary Pittsburgh sleep quality index (PSQI) Psychological questionnaire 4 weeks No
Secondary Depression score ( Zung's Self-Reported Depression Scale) Psychological questionnaire- Zung's Self-Reported Depression Scale 4 weeks No
Secondary Anxiety score (Beck Anxiety Inventory) Psychological questionnaire- Beck Anxiety Inventory 4 weeks No
Secondary Heart rate variability Cardiopulmonary functions 4 weeks No
Secondary Metabolic syndrome (NCEP) Third Report of the National Cholesterol Education Program (NCEP) criteria 4 weeks No
Secondary VCAM-1 Cardiovascular risk and Inflammatory markers 4 weeks No
Secondary Irisin Cardiovascular risk and Inflammatory markers 4 weeks No
Secondary circadian rhythm orexin 4 weeks No
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